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| 13C NMR (101 MHz, CDCl3) ¦Ä 199.84, 171.90, 138.26, 129.61, 123.87, 77.48, 77.16, 76.85, 56.16, 56.03, 53.97, 51.38, 45.98, 42.54, 42.42, 40.60, 39.77, 39.67, 38.97, 38.76, 36.26, 35.99, 35.83, 35.77, 34.12, 34.03, 33.79, 33.10, 32.56, 32.20, 32.01, 31.62, 31.05, 30.42, 29.84, 29.30, 29.00, 28.33, 26.23, 25.54, 24.39, 24.33, 23.22, 22.83, 21.30, 21.22, 21.18, 20.34, 19.96, 19.17, 19.13, 18.85, 18.77, 18.40, 17.53, 15.52, 14.25, 12.38, 12.29, 12.12, 12.09, 0.13. |
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ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
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2Â¥2015-05-07 15:48:04
874643370
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 18 (СѧÉú)
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ÅźÃÁË£º0.13,12.09,12.12,12.29,12.38,14.25,15.52,17.53,18.40,18.77, 18.85,19.13,19.17,19.96,20.34,21.18,21.22,21.30,22.83,23.22, 24.33,24.39,25.54,26.23,28.33,29.00,29.30,29.84,30.42, 31.05, 31.62,32.01,32.20,32.56,33.10,33.79,34.03,34.12, 35.77, 35.83, 35.99,36.26,38.76,38.97, 39.67,39.77,40.60,42.42, 42.54,45.98, 51.38,53.97, 56.03,56.16,76.85,77.16, 77.48,123.87,129.61, 138.26,171.90,199.84, |

3Â¥2015-05-07 19:24:21
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
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4Â¥2015-05-08 08:22:02
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
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- רҵ: ÌìÈ»Óлú»¯Ñ§
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874643370: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллÄú 2015-05-08 12:04:26
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874643370: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллÄú 2015-05-08 12:04:26
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1 . 4-Ethylcholesta-4,24(28)-dien-3-one C29H46O ÏàËÆ¶È:72.1% Chemistry of Natural Compounds 2011 Vol. 47, No. 3 465-466 POLYSACCHARIDES OF Fabaceae. VI. GALACTOMANNANS FROM SEEDS OF Astragalus alpinus AND A. tibetanus D. N. Olennikov and A. V. Rokhin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . ¦Â-sitosteryl acetate ÏàËÆ¶È:69.3% Chemical Communications 1978 319-320 Biosynthesis of ¦Â-sitosterol from [4-13C]mevalonic acid and sodium [1, 2-13C]acetate in tissue cultures of Isodon japonicus hara Shujiro Seo, Yutaka Tomita and Kazuo Tori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ¦Â-sitosterol and stigmasterol ÏàËÆ¶È:68.8% China Journal of Chinese Materia Medica 2001 26 692-694 Chemical Constituents of loxocalyx urticifolius Hemsl ZHANG Xiaorong, WANG Ming'an, ZHANG Yong, WANG Mingkui, IDNG Lisheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . sitosterol ÏàËÆ¶È:67.2% Chemical Communications 1986 1139-1140 Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from [2-13C, 2-2H3]Acetate Shujiro Seo, * Ushio Sankawa, Haruo Seto, Atsuko Uomori, Yohko Yoshimura, Yutaka Ebizuka, Hiroshi Noguchi, and Ken'ichi Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 7¦Â-tert-Butyldimethylsilyloxysitosteryl-9,10-ditert-butyldimethylsilyloxystearate C65H126O5Si3 ÏàËÆ¶È:65.5% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . N(2.8)-[ (tert-Butoxy)carbonyl][5-[4,4,4,4',4',4'-hexafluoro-N-(2-hydroxyethyoxy)-L-valine]]-7,8-secocyclosporin tert-Butyl Ester ÏàËÆ¶È:63.4% Helvetica Chimica Acta 2010 93 1583-1601 Stereoselective Synthesis of [5-[4,4,4,4¡ä,4¡ä,4¡ä-Hexafluoro-N-(2-hydroxyethoxy)-D-valine]]- and [5-[4,4,4,4¡ä,4¡ä,4¡ä-Hexafluoro-N-(2-hydroxyethoxy)-L-valine]cyclosporin A Marcel K. Eberle and Reinhart Keese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Cyclosporine D ÏàËÆ¶È:63.4% Helvetica Chimica Acta 1982 65 1655-1677 Isolierung und Strukturermittlung der neuen Cyclosporine E, F, G, H und I Ren¨¦ Traber, Hans-Rudolf Loosli, Hans Hofmann, Max Kuhn and Albert Von Wartburg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Cyclosporine G C63H113N11O12 ÏàËÆ¶È:63.4% Helvetica Chimica Acta 1982 65 1655-1677 Isolierung und Strukturermittlung der neuen Cyclosporine E, F, G, H und I Ren¨¦ Traber, Hans-Rudolf Loosli, Hans Hofmann, Max Kuhn and Albert Von Wartburg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Cyclosporin D ÏàËÆ¶È:63.4% Helvetica Chimica Acta 1987 70 13-36 Neue Cyclosporine aus Tolypocladium inflatum. Die Cyclosporine K¨CZ Ren¨¦ Traber, Hans Hofmann, Hans-Rudolf Loosli, Monique Ponelle and Albert von Wartburg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3¦Á-Hydroxy-7¦Á,12¦Á-bis(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oic acid C90H144O13 ÏàËÆ¶È:63.0% Steroids 2013 78 435-453 New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
5Â¥2015-05-08 08:22:20














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